Copper‐Catalyzed Borylative Methylation of Alkyl Iodides with CO as the C1 Source: Advantaged by Faster Reaction of CuH over CuBpin

CuH and CuBpin are versatile catalysts and intermediates in organic chemistry. However, studies that involve both CuH and CuBpin in the same reaction is still rarely reported due to their high reactivity. Now, a study on CuH‐ and CuBpin‐catalyzed borylative methylation of alkyl iodides with CO as th...

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Veröffentlicht in:Angewandte Chemie International Edition 2021-05, Vol.60 (21), p.11730-11734
Hauptverfasser: Wu, Fu‐Peng, Wu, Xiao‐Feng
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Sprache:eng
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Zusammenfassung:CuH and CuBpin are versatile catalysts and intermediates in organic chemistry. However, studies that involve both CuH and CuBpin in the same reaction is still rarely reported due to their high reactivity. Now, a study on CuH‐ and CuBpin‐catalyzed borylative methylation of alkyl iodides with CO as the C1 source is reported. Various one carbon prolongated alkyl boranes (RCH2Bpin and RCH(Bpin)2) were produced in moderate to good yields from the corresponding alkyl iodides (RI). In this cooperative system, CuH reacts with alkyl iodide faster than CuBpin. A study on CuH‐ and CuBpin‐catalyzed borylative methylation of alkyl iodides with CO as the C1 source is reported. Various one carbon prolongated alkyl boranes (RCH2Bpin and RCH(Bpin)2) were produced in moderate to good yields from the corresponding alkyl iodides (RI). In this cooperative system, CuH reacts with alkyl iodide faster than CuBpin.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.202102197